Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1150753 0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02 2
rs1748033 0.925 0.120 1 17336167 missense variant T/C;G snv 0.63; 4.0E-06 2
rs17581834 0.882 0.120 1 206802774 intron variant T/C snv 4.2E-02 3
rs1913517 0.925 0.120 10 48911009 intron variant A/G snv 0.54 2
rs204994 0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs2075876 0.925 0.120 21 44289270 non coding transcript exon variant G/A snv 0.19 2
rs2277798 0.925 0.120 21 42403997 missense variant A/G snv 0.55 0.60 3
rs2283790 0.882 0.120 22 21602364 intron variant A/G snv 0.21 3
rs3117103 0.925 0.120 6 32381780 intron variant A/T snv 9.6E-02 2
rs340630 0.925 0.120 4 87037243 intron variant G/A snv 0.42 2
rs34933034
CSK
0.925 0.120 15 74787133 intron variant G/A;T snv 3
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs4112788 0.851 0.120 1 152578800 downstream gene variant A/G;T snv 4
rs4921283 0.925 0.120 5 160443604 intron variant G/A snv 0.52 2
rs4937333 0.882 0.120 11 128460625 3 prime UTR variant T/C snv 0.45 4
rs494620 0.925 0.120 6 31870936 stop gained G/A;T snv 0.44; 4.1E-06 3
rs509749
LY9
0.925 0.120 1 160823770 missense variant A/G snv 0.54 0.55 2
rs6935269 0.925 0.120 6 32292573 intron variant T/C snv 0.25 2
rs704853 0.925 0.120 1 167499627 intron variant G/T snv 0.15 2
rs708035 0.925 0.120 3 10234479 missense variant T/A snv 0.73 0.70 2
rs7097397 0.925 0.120 10 48817351 missense variant G/A snv 0.38 0.31 2
rs7258015 0.925 0.120 19 10338682 missense variant T/C snv 0.22 0.20 2
rs771131230 0.925 0.120 6 32581827 missense variant C/A;T snv 2
rs773389640 0.925 0.120 6 32581821 missense variant C/G;T snv 2
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4